Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94430355G>T , CM000669.2:g.94430355G>T | GRCh38 |
| NC_000007.13:g.94059667G>T , CM000669.1:g.94059667G>T | GRCh37 |
| NC_000007.12:g.93897603G>T | NCBI36 |
| NG_007405.1:g.40795G>T , LRG_2:g.40795G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.4063G>T MANE Select | NP_000080.2:p.Glu1355Ter |
| ENST00000297268.11:c.4063G>T MANE Select | ENSP00000297268.6:p.Glu1355Ter |
| NM_000089.3:c.4063G>T , LRG_2t1:c.4063G>T | NP_000080.2:p.Glu1355Ter |
| ENST00000297268.10:c.4063G>T | ENSP00000297268.6:p.Glu1355Ter |
| ENST00000464916.1:n.1111G>T | |
| ENST00000481570.5:n.5660G>T | |
| ENST00000620463.1:c.4057G>T | ENSP00000477719.1:p.Glu1353Ter |